510(k) K151405
K151405 is an FDA 510(k) premarket notification submitted by Surgical Instrument Services and Savings(Dba Medline Renewal for the device "Medline ReNewal Reprocessed Harmonic ACE + Shears without Adaptive Tissue Technology". The FDA issued a decision of Substantially Equivalent on January 26, 2016. The device falls under product code NLQ (Single-Use Reprocessed Ultrasonic Surgical Instruments), a Class U device.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- January 26, 2016
- Date Received
- May 26, 2015
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Single-Use Reprocessed Ultrasonic Surgical Instruments
- Device Class
- Class U
- Regulation Number
- Review Panel
- SU
- Submission Type
Single-use reprocessed versions of the ultrasonic devices used in surgical procedures either for fragmentation, emulsification and aspiration of soft tissue and hard tissue or for ligation of vessels (under product code LFL). Reprocessing validation data for this device type must be included in a 510(k) submission.. (70 FR 56911, available at https://www.govinfo.gov/content/pkg/FR-2005-09-29/pdf/05-19510.pdf).